Hyperfine structure and higher nuclear moments by Schwartz, Charles Leon, 1931-

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Absence of mutations in <it>NR2E1 </it>and <it>SNX3 </it>in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes by Simpson Elizabeth M, Schwartz Charles E, Slavotinek Anne, Morgan Chad T, Everman David B, Kumar Ravinesh A

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TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation by Holinski-Feder Elke, Abramowicz Marc J, Gecz Jozef, Kooy Frank, Christophe-Hobertus Christiane, Schwartz Charles, Christophe Daniel

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The <it>FU </it>gene and its possible protein isoforms by Nöthen Markus M, Mosca Monica, Betz Regina C, Everman David B, Østerlund Torben, Schwartz Charles E, Zaphiropoulos Peter G, Toftgård Rune

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<it>DRD2</it> and <it>PPP1R1B</it> (<it>DARPP-32</it>) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in mal... by Hettinger Joe A, Liu Xudong, Hudson Melissa L, Lee Alana, Cohen Ira L, Michaelis Ron C, Schwartz Charles E, Lewis Suzanne ME, Holden Jeanette JA

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XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene by MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E

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Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C by Grafodatskaya Daria, Chung Barian HY, Butcher Darci T, Turinsky Andrei L, Goodman Sarah J, Choufani Sana, Chen Yi-An, Lou Youliang, Zhao Chunhua, Rajendram Rageen, Abidi Fatima E, Skinner Cindy, Stavropoulos James, Bondy Carolyn A, Hamilton Jill, Wodak Shoshana, Scherer Stephen W, Schwartz Charles E, Weksberg Rosanna

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